Medax’s Quality Management System is certified to ISO13485:2016 standards, in accordance with the requirements of the medical disposable 93/42/CEE directive and its relevant updates.
All products undergo intensive bench and clinical testing prior to market release.
All products are CE and FDA approved.
Medax, since its inception, has been focused on markets throughout the world, which has resulted in extensive product registration experience. Our Regulatory Department is committed to helping our customers registration efforts by applying our expertise throughout the product development process.
Medax Medical Devices India Private Limited
Registered Office: 602, Charkop, Mitashu Chs Ltd, R D P 6, Sector 6, Near TJSB Bank, Kandivali (W), Mumbai, 400067, Mumbai City, Maharashtra, India.
Warehouse: Shop No.1, Mahasagar Chs, Plot No. 112, Sector No.4, Opp Haryana Bhavan, Charkop,Kandivali West , Mumbai 400067, Maharashtra, India. - This email address is being protected from spambots. You need JavaScript enabled to view it.
MEDAX S.R.L. Unipersonale
Via Sandro Pertini, 4 - 41039 - San Possidonio (MO) - Italy
Company direct No. : +39 0535 1812757 This email address is being protected from spambots. You need JavaScript enabled to view it.
Vat N. /Fiscal Code N. Iscriz. Reg. Impr. 02669860369 - N. REA: MO 403036 - Capitale Sociale Euro 100.011,00 i.v.
In accordance with the requirements of the medical device 93/42/EEC directive and its relevant updates. All products undergo intensive clinical testing and are fully EC and FDA approved.
